A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334208



Internal ID20867391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180629001..180633700hg38UCSC Ensembl
chr1:180598137..180602836hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201721
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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